Search Results - Puel, Mathilde

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  1. 1
    Redefining tryptase norms in the pediatric population reveals sex-based differences: Clinical implications

    Redefining tryptase norms in the pediatric population reveals sex-based differences: Clinical implications by Puel, Mathilde, Rossignol, Julien, Devin, Clotilde, Madrange, Marine, Diep, Antoine, Roland, Pascale Nicaise, Chollet-Martin, Sylvie, Husson, Julien, Hermine, Olivier, Bodemer, Christine, Brouzes, Chantal, De Chaisemartin, Luc, Polivka, Laura

    Published in Allergy (Copenhagen)
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  2. 2
    2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 Deficiency

    2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 Deficiency by Brakta, Charlyne, Tabet, Anne-Claude, Puel, Mathilde, Pacault, Mathilde, Stolzenberg, Marie-Claude, Goudet, Claire, Merger, Marguerite, Reumaux, Héloïse, Lambert, Nathalie, Alioua, Najiba, Malan, Valérie, Hanein, Sylvain, Dupin-Deguine, Delphine, Treiner, Emmanuel, Lefèvre, Guillaume, Farhat, Méryem-Maud, Luca, Luminita Elena, Hureaux, Marguerite, Li, Hailun, Chelloug, Nora, Dehak, Rabha, Boussion, Simon, Ouachée-Chardin, Marie, Schleinitz, Nicolas, Abou Chahla, Wadih, Barlogis, Vincent, Vély, Frédéric, Oksenhendler, Eric, Quartier, Pierre, Pasquet, Marlène, Suarez, Felipe, Bustamante, Jacinta, Neven, Bénédicte, Picard, Capucine, Rieux-Laucat, Frédéric, Lévy, Jonathan, Rosain, Jérémie

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  3. 3
    Imbalance between alpha-1-antitrypsin and interleukin 6 is associated with in-hospital mortality and thrombosis during COVID-19

    Imbalance between alpha-1-antitrypsin and interleukin 6 is associated with in-hospital mortality and thrombosis during COVID-19 by Philippe, Aurélien, Puel, Mathilde, Narjoz, Céline, Gendron, Nicolas, Durey-Dragon, Marie Agnès, Vedie, Benoit, Balduyck, Malika, Chocron, Richard, Hauw-Berlemont, Caroline, Sanchez, Olivier, Mirault, Tristan, Diehl, Jean-Luc, Smadja, David M., Loriot, Marie Anne

    Published in Biochimie
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  4. 4
    New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome

    New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome by Arlabosse, Tiphaine, Materna, Marie, Riccio, Orbicia, Schnider, Caroline, Angelini, Federica, Perreau, Matthieu, Rochat, Isabelle, Superti-Furga, Andrea, Campos-Xavier, Belinda, Héritier, Sébastien, Pereira, Anaïs, Deswarte, Caroline, Lévy, Romain, Distefano, Marco, Bustamante, Jacinta, Roelens, Marie, Borie, Raphaël, Le Brun, Mathilde, Crestani, Bruno, Casanova, Jean-Laurent, Puel, Anne, Hofer, Michaël, Fieschi, Claire, Theodoropoulou, Katerina, Béziat, Vivien, Candotti, Fabio

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  5. 5
    Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome

    Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome by Arlabosse, Tiphaine, Materna, Marie, Riccio, Orbicia, Schnider, Caroline, Angelini, Federica, Perreau, Matthieu, Rochat, Isabelle, Superti-Furga, Andrea, Campos-Xavier, Belinda, Héritier, Sébastien, Pereira, Anaïs, Deswarte, Caroline, Lévy, Romain, Distefano, Marco, Bustamante, Jacinta, Roelens, Marie, Borie, Raphaël, Le Brun, Mathilde, Crestani, Bruno, Casanova, Jean‑Laurent, Puel, Anne, Hofer, Michaël, Fieschi, Claire, Theodoropoulou, Katerina, Béziat, Vivien, Candotti, Fabio

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  6. 6
    Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

    Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons by Bolze, Alexandre, Boisson, Bertrand, Bosch, Barbara, Antipenko, Alexander, Bouaziz, Matthieu, Sackstein, Paul, Chaker-Margot, Malik, Barlogis, Vincent, Briggs, Tracy, Colino, Elena, Elmore, Aurora C., Fischer, Alain, Genel, Ferah, Hewlett, Angela, Jedidi, Maher, Kelecic, Jadranka, Krüger, Renate, Ku, Cheng-Lung, Kumararatne, Dinakantha, Lefevre-Utile, Alain, Loughlin, Sam, Mahlaoui, Nizar, Markus, Susanne, Garcia, Juan-Miguel, Nizon, Mathilde, Oleastro, Matias, Pac, Malgorzata, Picard, Capucine, Pollard, Andrew J., Rodriguez-Gallego, Carlos, Thomas, Caroline, Von Bernuth, Horst, Worth, Austen, Meyts, Isabelle, Risolino, Maurizio, Selleri, Licia, Puel, Anne, Klinge, Sebastian, Abel, Laurent, Casanova, Jean-Laurent

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  7. 7
    A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease

    A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease by ROVELET-LECRUX, Anne, LEGALLIC, Solenn, PUEL, Michele, PAQUET, Claire, CROISILE, Bernard, THOMAS-ANTERION, Catherine, VERCELLETTO, Martine, LEVY, Richard, FREBOURG, Thierry, HANNEQUIN, Didier, CAMPION, Dominique, WALLON, David, FLAMAN, Jean-Michel, MARTINAUD, Olivier, BOMBOIS, Stéphanie, ROLLIN-SILLAIRE, Adeline, MICHON, Agnes, LE BER, Isabelle, PARIENTE, Jérémie

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  8. 8
    Diffuse Endocapillary Glomerulonephritis in a Child With IL-17RA Deficiency Emphasizes the Pivotal Role of the Complement Cascade and Anaphylatoxins

    Diffuse Endocapillary Glomerulonephritis in a Child With IL-17RA Deficiency Emphasizes the Pivotal Role of the Complement Cascade and Anaphylatoxins by d’Izarny-Gargas, Thibaut, Grapin, Mathilde, Grunenwald, Anne, Duong-Van-Huyen, Jean-Paul, Rabant, Marion, Lévy, Romain, Puel, Anne, Toubiana, Julie, Boyer, Olivia, Frémeaux-Bacchi, Véronique, Charbit, Marina, Isnard, Pierre

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  9. 9
    Diffuse Endocapillary Glomerulonephritis in a Child With IL-17RA Deficiency Emphasizes the Pivotal Role of the Complement Cascade and Anaphylatoxins

    Diffuse Endocapillary Glomerulonephritis in a Child With IL-17RA Deficiency Emphasizes the Pivotal Role of the Complement Cascade and Anaphylatoxins by d'Izarny-Gargas, Thibaut, Grapin, Mathilde, Grunenwald, Anne, Duong-Van-Huyen, Jean-Paul, Rabant, Marion, Lévy, Romain, Puel, Anne, Toubiana, Julie, Boyer, Olivia, Frémeaux-Bacchi, Véronique, Charbit, Marina, Isnard, Pierre

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